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CYBERWHITE EX
CYBERWHITE EX - 11559-004-01 - (OCTINOXATE, OCTISALATE, ZINC OXIDE, OXYBENZONE, TITANIUM DIOXIDE)
Drug Information of CYBERWHITE EX
| Product NDC: | 11559-004 |
| Proprietary Name: | CYBERWHITE EX |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, ZINC OXIDE, OXYBENZONE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 7.5; 4; 2.5; 1.1; 3.5 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, ZINC OXIDE, OXYBENZONE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CYBERWHITE EX
| Product NDC: | 11559-004 |
| Labeler Name: | ESTEE LAUDER INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100201 |
Package Information of CYBERWHITE EX
| Package NDC: | 11559-004-01 |
| Package Description: | 1 TUBE in 1 CARTON (11559-004-01) > 50 mL in 1 TUBE (11559-004-02) |
NDC Information of CYBERWHITE EX
| NDC Code | 11559-004-01 |
| Proprietary Name | CYBERWHITE EX |
| Package Description | 1 TUBE in 1 CARTON (11559-004-01) > 50 mL in 1 TUBE (11559-004-02) |
| Product NDC | 11559-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, ZINC OXIDE, OXYBENZONE, TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ESTEE LAUDER INC |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7.5; 4; 2.5; 1.1; 3.5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
